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MEDRAD® Mark V ProVis 200mL FasTurn Sterile Disposable Syringe & QFT

FDA UDI

Class II (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name
MEDRAD® Mark V ProVis 200mL FasTurn Sterile Disposable Syringe & QFT FDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
PROVIS,KIT,SYR,ANGIO,200ML,MC,WLD (86617560) FDA UDI
Model / Reference
200-FT-Q FDA UDI
Description
PROVIS,KIT,SYR,ANGIO,200ML,MC,WLD (86617560) FDA UDI

Identifiers

Catalog Number
200-FT-Q FDA UDI
Primary DI / UDI-DI
00616258021812 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiographic syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Angiographic syringe

MEDRAD® Mark V ProVis 200mL FasTurn Sterile Disposable Syringe & QFT by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Angiographic syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 09a71467-9661-4d70-bc19-d5b7c6db2cbe 35 fields · synced Jun 9, 2026